STX10 Rabbit Polyclonal Antibody, 50ul Low-speed Centrifuges and mutations in the gene

and mutations in the gene are the cause of 17beta-hydroxysteroid dehydrogenase type 10 (HSD10) deficiency

This gene was previously referred to as ANGPTL2 but has been renamed ANGPTL4

Defects in this gene are associated with idiopathic growth retardation and in the short stature phenotype of Turner syndrome patients

and is found to be involved in transducing the proliferating signals in normal diploid fibroblast and T cells

and has been shown to inhibit NF-kappa B activation as well as TNF-mediated apoptosis

STX10 Rabbit Polyclonal Antibody, 50ul Low-speed Centrifuges and mutations in the geneThis gene belongs to the syntaxin family and encodes a soluble N ethylmaleimide sensitive factor attachment protein receptor (SNARE). The encoded protein is involved in docking and fusion events at the Golgi apparatus. Alternative splicing results in multiple transcript variants.